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Cancer Genetics and Cytogenetics|December 2, 2004
Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancerJean-Marc Rey, Mehrdad Noruzinia, Jean-Paul Brouillet, et al.
Human Mutation|March 1, 2019
Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndromeJérôme Solassol, Marion Larrieux, Julie Leclerc, et al.
The Journal of Molecular Diagnostics : JMD|May 16, 2017
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation SequencingJean-Marc Rey, Vincent Ducros, Pascal Pujol, et al.
Bulletin Du Cancer|May 23, 2002
[Genetic alterations of transcription cofactors in solid tumors]Jean-François Rouayrenc, Audrey Castet, Jean-Marc Rey, et al.
European Journal of Medical Genetics|December 26, 2021
A novel POLD1 pathogenic variant identified in two families with a cancer spectrum mimicking Lynch syndromeClémentine Legrand, Marine Lebrun, Pierre Naïbo, et al.
Psycho-Oncology|June 2, 2019
Psychosocial and clinical factors of probands impacting intrafamilial disclosure and uptake of genetic testing among families with BRCA1/2 or MMR gene mutationsNathalie Alegre, Pierre Vande Perre, Yves Jean Bignon, et al.
Breast Cancer Research and Treatment|August 6, 2017
Early onset breast cancer: differences in risk factors, tumor phenotype, and genotype between North African and South European womenCarole Corsini, Sarra Henouda, Dalel Ben Nejima, et al.
Thyroid : Official Journal of the American Thyroid Association|September 27, 2017
Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as ModifiersMaylis Lebeault, Stéphane Pinson, Marine Guillaud-Bataille, et al.
Clinical Genetics|January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.
European Journal of Human Genetics : EJHG|August 10, 2018
Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendationsPascal Pujol, Pierre Vande Perre, Laurence Faivre, et al.
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